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木蛙在冷冻暴露期间的信号转导、第二信使和蛋白激酶反应。

Signal transduction, second messenger, and protein kinase responses during freezing exposures in wood frogs.

作者信息

Holden C P, Storey K B

机构信息

Institute of Biochemistry, Carleton University, Ottawa, Ontario, Canada.

出版信息

Am J Physiol. 1996 Nov;271(5 Pt 2):R1205-11. doi: 10.1152/ajpregu.1996.271.5.R1205.

Abstract

Changes in the percentage of adenosine 3', 5'-cyclic monophosphate (cAMP)-dependent protein kinase present as the active catalytic subunit (PKAc) and in the levels of the second messengers cAMP, guanosine 3',5'-cyclic monophosphate (cGMP), and D-myo-inositol 1,4,5-trisphosphate (IP3) were quantified in tissues of the freeze-tolerant wood frog Rana sylvatica over the course of freezing at -2.5 degrees C and thawing at 5 degrees C. Freezing exposure rapidly raised liver cAMP concentration and %PKAc (by 2- and 6-fold, respectively) within 2 min postnucleation; both peaked and stabilized between 5 and 60 min postnucleation but declined with longer freezing. Other organs also showed elevated PKAc during freezing, particularly skeletal muscle. By contrast, cGMP concentration was reduced in muscle and kidney after 24 h of freezing but rose after thawing in muscle. Liver also showed a twofold elevation of cGMP during thawing. The protein kinase C (PKC) second messenger, IP3, rose throughout freezing in liver, reaching levels 11-fold higher than control values after 24 h of freezing. IP3 was also elevated in brain after 4 and 8 h of freezing. The different patterns of cAMP, protein kinase A (PKA), and IP3 changes in liver suggest that, whereas cAMP and PKA clearly mediate the rapid activation of glucose output as a cryoprotectant, IP3 and PKC may be involved instead with metabolic responses that deal with the consequences of long-term freezing, such as ischemia resistance or cell volume control.

摘要

在耐冻的林蛙(Rana sylvatica)组织中,对以活性催化亚基(PKAc)形式存在的3',5'-环磷酸腺苷(cAMP)依赖性蛋白激酶的百分比变化以及第二信使cAMP、3',5'-环磷酸鸟苷(cGMP)和D-肌醇1,4,5-三磷酸(IP3)的水平,在-2.5℃冷冻和5℃解冻过程中进行了定量分析。冷冻暴露在成核后2分钟内迅速提高了肝脏cAMP浓度和PKAc百分比(分别提高了2倍和6倍);两者在成核后5至60分钟达到峰值并稳定下来,但随着冷冻时间延长而下降。其他器官在冷冻期间PKAc也升高,尤其是骨骼肌。相比之下,冷冻24小时后肌肉和肾脏中的cGMP浓度降低,但解冻后肌肉中的cGMP浓度升高。解冻期间肝脏中的cGMP也升高了两倍。蛋白激酶C(PKC)的第二信使IP3在肝脏冷冻过程中持续升高,冷冻24小时后达到比对照值高11倍的水平。冷冻4小时和8小时后大脑中的IP3也升高。肝脏中cAMP、蛋白激酶A(PKA)和IP3的不同变化模式表明,虽然cAMP和PKA显然介导了作为冷冻保护剂的葡萄糖输出的快速激活,但IP3和PKC可能反而参与了应对长期冷冻后果的代谢反应,如缺血抗性或细胞体积控制。

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